A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001097



Internal ID7066226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:30465297..30475494hg38UCSC Ensembl
Outerchr4:30466919..30477116hg19UCSC Ensembl
Outerchr4:30076017..30086214hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810198
hg1910198
hg1810198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563859
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001097
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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